CYP93A2

Glycine max CYP93A

Fabaceae

Substrate reaction site Product reaction site MCS substructure diff highlighting · RDKit atom mapping

Substrate

3,9-dihydroxypterocarpan

PubChem ↗ C1[C@@H]2[C@H](C3=C(O1)C=C(C=C3)O)OC4=C2C=CC(=C4)O

CYP93A2

ΔMass: -2.0157 Da ketone_formation(-2.0157)

Product

daidzein

PubChem ↗ C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)O

Evidence trail

Excerpts are machine-extracted plain text for biochemical provenance. Follow DOI / PubMed links for the primary literature; publisher figures and PDF images are not displayed here.

Source text excerpt ation; ation; Glycine max; higher catalytic efficiency for daidzein production.

Reaction & quality gates

Mechanism: Ketone formation (-2.02 Da)
Evidence type: In vitro
Confidence: High
Data tier: Quarantine
PDF audit quarantine (enzyme_miss_in_pdf;two_core_fields_in_text;review_structured_partial_core). pdf=41799975.pdf; enzyme_in_pdf=miss; issue=review_structured…
Substrate class: Other
Product class: Other

Literature & public identifiers

PubMed: PMID:41799975 ↗
DOI: 10.3389/fpls.2026.1765290 ↗
UniProt: Q42799 ↗
GenBank: —
NCBI TaxID: 3847 ↗

Cytochrome P450 gene family: cross-pathway functional conservation, novel catalytic reactions, and synthetic biology-driven applications in plant secondary metabolism.

Evidence trail

Reaction & quality gates

Literature & public identifiers

Other reactions by this enzyme